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Xavier Zanlonghi

Showing results (11-20 of 58) with videos related to

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American Journal of Ophthalmology|February 3, 2009
Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entityChristian P Hamel, Isabelle Meunier, Carl Arndt, et al.
Human Mutation|October 21, 2018
Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analysesChristel Vaché, Simona Torriano, Valérie Faugère, et al.
Scientific Reports|September 22, 2021
Characterization of SSBP1-related optic atrophy and foveopathyIsabelle Meunier, Béatrice Bocquet, Sabine Defoort-Dhellemmes, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Genes|March 6, 2021
Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic <i>RPGRIP1</i> Pathologic Variant in the French Leber Congenital Amaurosis CohortIsabelle Perrault, Sylvain Hanein, Xavier Gérard, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Molecular Neurodegeneration|February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathyMajida Charif, Yvette C Wong, Soojin Kim, et al.
Orphanet Journal of Rare Diseases|February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathyStéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
Ophthalmology and Therapy|January 1, 2023
LIGHTSITE II Randomized Multicenter Trial: Evaluation of Multiwavelength Photobiomodulation in Non-exudative Age-Related Macular DegenerationBen Burton, Maurizio Battaglia Parodi, Ignasi Jürgens, et al.
Ophthalmology|August 3, 2014
Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genesIsabelle Meunier, Gaël Manes, Béatrice Bocquet, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Ophthalmology|February 3, 2009
Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entityChristian P Hamel, Isabelle Meunier, Carl Arndt, et al.
Human Mutation|October 21, 2018
Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analysesChristel Vaché, Simona Torriano, Valérie Faugère, et al.
Scientific Reports|September 22, 2021
Characterization of SSBP1-related optic atrophy and foveopathyIsabelle Meunier, Béatrice Bocquet, Sabine Defoort-Dhellemmes, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Genes|March 6, 2021
Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic <i>RPGRIP1</i> Pathologic Variant in the French Leber Congenital Amaurosis CohortIsabelle Perrault, Sylvain Hanein, Xavier Gérard, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Molecular Neurodegeneration|February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathyMajida Charif, Yvette C Wong, Soojin Kim, et al.
Orphanet Journal of Rare Diseases|February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathyStéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
Ophthalmology and Therapy|January 1, 2023
LIGHTSITE II Randomized Multicenter Trial: Evaluation of Multiwavelength Photobiomodulation in Non-exudative Age-Related Macular DegenerationBen Burton, Maurizio Battaglia Parodi, Ignasi Jürgens, et al.
Ophthalmology|August 3, 2014
Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genesIsabelle Meunier, Gaël Manes, Béatrice Bocquet, et al.
Pageof 6